ID: ALA482040

Max Phase: Preclinical

Molecular Formula: C15H22O2

Molecular Weight: 234.34

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@@H]1CCC2=C3C1=COC[C@@]3(C)[C@H](O)C2(C)C

Standard InChI:  InChI=1S/C15H22O2/c1-9-5-6-11-12-10(9)7-17-8-15(12,4)13(16)14(11,2)3/h7,9,13,16H,5-6,8H2,1-4H3/t9-,13-,15-/m1/s1

Standard InChI Key:  FMUFYIFXWSUYSC-XXLQHYSLSA-N

Associated Targets(non-human)

[Chlorella] fusca 158 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Priestia megaterium 1154 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Microbotryum violaceum 192 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 234.34Molecular Weight (Monoisotopic): 234.1620AlogP: 3.03#Rotatable Bonds: 0
Polar Surface Area: 29.46Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.86CX LogD: 1.86
Aromatic Rings: 0Heavy Atoms: 17QED Weighted: 0.70Np Likeness Score: 2.99

References

1. Krohn K, Dai J, Flörke U, Aust HJ, Dräger S, Schulz B..  (2005)  Botryane metabolites from the fungus Geniculosporium sp. isolated from the marine red alga Polysiphonia.,  68  (3): [PMID:15787444] [10.1021/np0498206]

Source